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rs587781506

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781506(A;A)
Make rs587781506(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32362594
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587781506
ebirs587781506
HLIrs587781506
Exacrs587781506
Varsomers587781506
Maprs587781506
PheGenIrs587781506
hapmaprs587781506
1000 genomesrs587781506
hgdprs587781506
ensemblrs587781506
gopubmedrs587781506
geneviewrs587781506
scholarrs587781506
googlers587781506
pharmgkbrs587781506
gwascentralrs587781506
openSNPrs587781506
23andMers587781506
23andMe allrs587781506
SNP Nexus

SNPshotrs587781506
SNPdbers587781506
MSV3drs587781506
GWAS Ctlgrs587781506
Max Magnitude0
ClinVar
Risk rs587781506(A;A)
Alt rs587781506(A;A)
Reference rs587781506(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32936731G>A
CLNSRC
CLNACC RCV000129483.2, RCV000195555.2,